Potassium Acetate
- Product NDC
- 65219-510
- 11-digit product format
- 652190510
- Labeler code
- 65219
- Product ID
- 65219-510_67c83f58-73cd-47d2-8dbc-e0fd8331c6e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM ACETATE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA217515
- Marketing category
- ANDA
- Marketing start
- 2024-11-27
- Substance
- POTASSIUM ACETATE
- Active strength
- 3.93 g/20mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| M911911U02 | POTASSIUM ACETATE | 127-08-2 | POTASSIUM ACETATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 65219-510-20 | 65219051020 | 25 VIAL, SINGLE-DOSE in 1 TRAY (65219-510-20) / 20 mL in 1 VIAL, SINGLE-DOSE (65219-510-02) | 2024-11-27 | No | No | Historical |